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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Investigation of the correlation between chemical structure and morphology in oligoaniline microspheres produced in buffered conditions

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Autor(es):
dos Santos, Isabela F. S. [1] ; Temperini, Marcia L. A. [1]
Número total de Autores: 2
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Inst Chem, Dept Fundamental Chem, Av Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: EUROPEAN POLYMER JOURNAL; v. 122, JAN 5 2020.
Citações Web of Science: 0
Resumo

Although the mainly intermolecular forces involved in the self-assembly of oligoaniline molecules have been consistently discussed (hydrogen bonds and pi-pi stacking interactions) the correlation between the driving forces and the large variations of morphology that can be obtained is still open in discussion, mostly because a detailed chemical characterization of such products is usually difficult to achieve. In this work, 3-D fluorescence spectroscopy is presented as a powerful technique in the identification and differentiation of phenazinic segments, with Raman spectroscopy being crucial for identification of 1,4-Michael-type segments and the verification of non-hydrolyzed imine groups in oligoaniline microspheres produced under pH 4.5 buffered conditions and employing different reagent concentrations. The results suggested that the self-assembly must occur by hydrogen bonds related to the non-hydrolyzed iminic groups and pi-pi stacking interactions between non-substituted phenazinic segments. Moreover, obtaining specific morphologies (flower-like structures, porous microspheres and hollow microspheres) showed dependence with the increase of the relative reagent concentrations. (AU)

Processo FAPESP: 16/21070-5 - Espectroscopia vibracional com resolução espacial
Beneficiário:Mauro Carlos Costa Ribeiro
Modalidade de apoio: Auxílio à Pesquisa - Temático